Variant report

Variant	nsv870807
Chromosome Location	chr1:78867347-79032598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:79019684-79019805	HepG2	liver:	n/a	n/a
2	BACH1	chr1:78956695-78956832	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr1:79027250-79027578	GM12878	blood:	n/a	chr1:79027451-79027460
4	BHLHE40	chr1:78917853-78917854	GM12878	blood:	n/a	n/a
5	BRCA1	chr1:78938626-78938807	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr1:78890922-78890931	GM12878	blood:	n/a	n/a
7	CEBPB	chr1:78958948-78959508	IMR90	lung:	n/a	chr1:78959078-78959089
8	CEBPB	chr1:78980629-78980818	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:79002123-79002542	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:78941902-78942305	Hela-S3	cervix:	n/a	chr1:78942101-78942112 chr1:78942078-78942089
11	CEBPB	chr1:78941989-78942241	HepG2	liver:	n/a	chr1:78942101-78942112 chr1:78942078-78942089
12	CEBPB	chr1:78980756-78980852	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:78980624-78980903	A549	lung:	n/a	n/a
14	CEBPB	chr1:78937221-78939197	Hela-S3	cervix:	n/a	chr1:78938931-78938942
15	CEBPB	chr1:78938789-78939089	HepG2	liver:	n/a	chr1:78938931-78938942
16	CEBPB	chr1:78927369-78927451	A549	lung:	n/a	n/a
17	CEBPB	chr1:78957203-78957393	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:79027252-79027486	HepG2	liver:	n/a	chr1:79027410-79027419 chr1:79027408-79027421 chr1:79027408-79027419 chr1:79027410-79027421
19	CEBPB	chr1:78958167-78958317	K562	blood:	n/a	chr1:78958228-78958239
20	CEBPB	chr1:78930370-78930599	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:78958090-78958382	A549	lung:	n/a	chr1:78958228-78958239
22	CEBPB	chr1:78975377-78975421	IMR90	lung:	n/a	chr1:78975405-78975416
23	CEBPB	chr1:78958055-78958424	IMR90	lung:	n/a	chr1:78958228-78958239
24	CEBPB	chr1:78941959-78942301	HepG2	liver:	n/a	chr1:78942101-78942112 chr1:78942078-78942089
25	CEBPB	chr1:78941928-78942252	IMR90	lung:	n/a	chr1:78942101-78942112 chr1:78942078-78942089
26	CEBPB	chr1:78980621-78980946	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:79002917-79003279	IMR90	lung:	n/a	chr1:79003096-79003107
28	CEBPB	chr1:78941791-78942298	HepG2	liver:	n/a	chr1:78942101-78942112 chr1:78942078-78942089
29	CEBPB	chr1:79002996-79003254	K562	blood:	n/a	chr1:79003096-79003107
30	CEBPB	chr1:78941932-78942212	A549	lung:	n/a	chr1:78942101-78942112 chr1:78942078-78942089
31	CEBPB	chr1:78938865-78939151	MCF-7	breast:	n/a	chr1:78938931-78938942
32	CEBPB	chr1:79019631-79019908	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:78974940-78975161	HepG2	liver:	n/a	chr1:78975016-78975027
34	CEBPB	chr1:78958070-78958411	HepG2	liver:	n/a	chr1:78958228-78958239
35	CEBPB	chr1:79003910-79004133	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:78958134-78958387	H1-hESC	embryonic stem cell:	n/a	chr1:78958228-78958239
37	CEBPB	chr1:78981913-78982140	HepG2	liver:	n/a	chr1:78981993-78982002 chr1:78981991-78982002
38	CEBPB	chr1:78938779-78939116	IMR90	lung:	n/a	chr1:78938931-78938942
39	CEBPB	chr1:79003979-79004169	A549	lung:	n/a	n/a
40	CEBPB	chr1:78958924-78959199	HepG2	liver:	n/a	chr1:78959078-78959089
41	CEBPB	chr1:79002970-79003227	H1-hESC	embryonic stem cell:	n/a	chr1:79003096-79003107
42	CEBPB	chr1:78907559-78907963	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:78938826-78939105	A549	lung:	n/a	chr1:78938931-78938942
44	CEBPB	chr1:79001040-79001248	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:79002941-79003279	HepG2	liver:	n/a	chr1:79003096-79003107
46	CEBPB	chr1:78941929-78942302	HepG2	liver:	n/a	chr1:78942101-78942112 chr1:78942078-78942089
47	CEBPB	chr1:78888820-78889033	HepG2	liver:	n/a	chr1:78888887-78888898
48	CEBPB	chr1:79002963-79003252	A549	lung:	n/a	chr1:79003096-79003107
49	CHD1	chr1:78957152-78957158	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr1:78956542-78956767	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:78956847-78956897	HRCEpiC	kidney:	n/a
2	chr1:78960610-78960660	GM19239	blood:	n/a
3	chr1:78956847-78956897	HRCEpiC	kidney:	n/a
4	chr1:78960610-78960660	GM19239	blood:	n/a
5	chr1:78957682-78957732	U87	brain:	n/a
6	chr1:78956570-78956620	NHBE	bronchial:	n/a
7	chr1:78957515-78957565	AG04449	skin:	fetal
8	chr1:78956905-78956955	NH-A	brain:	n/a
9	chr1:78956458-78956508	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:78957515-78957565	H1-hESC	embryonic stem cell:	embryo
11	chr1:78956570-78956620	GM19239	blood:	n/a
12	chr1:78957203-78957253	HEK293	kidney:	embryo
13	chr1:78956847-78956897	MCF-7	breast:	n/a
14	chr1:78957515-78957565	HL-60	blood:	n/a
15	chr1:78960610-78960660	NH-A	brain:	n/a
16	chr1:78956845-78956895	MCF-7	breast:	n/a
17	chr1:78892408-78892458	A549	lung:	n/a
18	chr1:78956268-78956318	GM19239	blood:	n/a
19	chr1:78956905-78956955	SK-N-SH_RA	brain:	n/a
20	chr1:78957682-78957732	RPTEC	kidney:	n/a
21	chr1:78956845-78956895	AoSMC	blood vessel:	n/a
22	chr1:78957253-78957303	HCM	heart:	n/a
23	chr1:78957253-78957303	AoSMC	blood vessel:	n/a
24	chr1:78956268-78956318	HCM	heart:	n/a
25	chr1:78956845-78956895	GM12892	blood:	n/a
26	chr1:78957203-78957253	AG10803	skin:	n/a
27	chr1:78956845-78956895	Jurkat	blood:	n/a
28	chr1:78892408-78892458	AG04450	lung:	fetal
29	chr1:78957253-78957303	MCF10A-Er-Src	breast:	n/a
30	chr1:78956845-78956895	NHBE	bronchial:	n/a
31	chr1:78956905-78956955	HRE	kidney:	n/a
32	chr1:78960610-78960660	HNPCEpiC	eye:	n/a
33	chr1:78956268-78956318	SK-N-MC	brain:	n/a
34	chr1:78892408-78892458	MCF-7	breast:	n/a
35	chr1:78892408-78892458	PFSK-1	brain:	n/a
36	chr1:78957253-78957303	AG10803	skin:	n/a
37	chr1:78957203-78957253	HUVEC	blood vessel:	n/a
38	chr1:78957203-78957253	LNCaP	prostate:	n/a
39	chr1:78956905-78956955	NB4	blood:	n/a
40	chr1:78957515-78957565	T-47D	breast:	n/a
41	chr1:78956458-78956508	HCM	heart:	n/a
42	chr1:78957682-78957732	Hepatocyte	liver:	n/a
43	chr1:78956458-78956508	SK-N-SH_RA	brain:	n/a
44	chr1:78956458-78956508	HEK293	kidney:	embryo
45	chr1:78957203-78957253	Hela-S3	cervix:	n/a
46	chr1:78960610-78960660	SK-N-MC	brain:	n/a
47	chr1:78956845-78956895	SKMC	muscle:	n/a
48	chr1:78956570-78956620	HRPEpiC	eye:	n/a
49	chr1:78956268-78956318	HEEpiC	esophagus:	n/a
50	chr1:78956847-78956897	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:78953624..78955223-chr1:78965272..78967334,2	K562	blood:
2	chr1:78913260..78915491-chr1:78917336..78919213,2	K562	blood:
3	chr1:78913260..78915491-chr1:78917336..78919213,2	K562	blood:
4	chr1:78953624..78955223-chr1:78965272..78967334,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTGFR	hsa-miR-21-5p	chr1:79002228-79002246

Variant related genes	Relation type
PTGFR	TF binding region
PTGFR	CpG island

Extended variants
information (count: 5737 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:5737 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs487376	chr1:78867347-78867348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369686287	chr1:78867370-78867371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373437342	chr1:78867373-78867374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531181342	chr1:78867393-78867394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372879183	chr1:78867394-78867395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569645939	chr1:78867403-78867404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149943472	chr1:78867404-78867405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573720690	chr1:78867443-78867444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555212566	chr1:78867532-78867533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1333069	chr1:78867541-78867542	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs190869191	chr1:78867560-78867561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554241917	chr1:78867562-78867563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200338995	chr1:78867620-78867621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377131739	chr1:78867621-78867622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572444598	chr1:78867765-78867766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181965697	chr1:78867781-78867782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs491295	chr1:78867799-78867800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs576359803	chr1:78867828-78867829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78079110	chr1:78867908-78867909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115119361	chr1:78867953-78867954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375655950	chr1:78868068-78868069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145081479	chr1:78868114-78868115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370489190	chr1:78868117-78868118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148692537	chr1:78868145-78868146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559448814	chr1:78868225-78868226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186529153	chr1:78868282-78868283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550998671	chr1:78868294-78868295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189788741	chr1:78868323-78868324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530399434	chr1:78868374-78868375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373937438	chr1:78868392-78868393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144150966	chr1:78868420-78868421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182453328	chr1:78868426-78868427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534859568	chr1:78868431-78868432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368365067	chr1:78868468-78868469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565345138	chr1:78868532-78868533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546475113	chr1:78868559-78868560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532994558	chr1:78868612-78868613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188252105	chr1:78868653-78868654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs494981	chr1:78868658-78868659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs558248060	chr1:78868659-78868660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374244734	chr1:78868822-78868823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191209994	chr1:78868843-78868844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537395436	chr1:78868845-78868846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183506743	chr1:78868846-78868847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574239741	chr1:78868868-78868869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562375598	chr1:78868882-78868883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188446791	chr1:78868954-78868955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79870769	chr1:78868991-78868992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528878864	chr1:78869015-78869016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544727177	chr1:78869023-78869024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:803 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78862400-78874600	Weak transcription	Fetal Muscle Leg	muscle
2	chr1:78868000-78868200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:78868200-78879600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:78873400-78874200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:78873400-78875400	Enhancers	NHDF-Ad	bronchial
6	chr1:78873800-78874800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:78874200-78874600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:78874200-78875000	Enhancers	Osteobl	bone
9	chr1:78874200-78875200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:78874400-78874800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:78874400-78875000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:78874600-78875000	Enhancers	Fetal Muscle Leg	muscle
13	chr1:78874600-78875200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:78874600-78875400	Enhancers	Fetal Muscle Trunk	muscle
15	chr1:78874600-78875600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:78875000-78875600	Weak transcription	Fetal Muscle Leg	muscle
17	chr1:78875400-78875600	Weak transcription	Fetal Muscle Trunk	muscle
18	chr1:78875600-78876400	ZNF genes & repeats	Fetal Muscle Leg	muscle
19	chr1:78875600-78876600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
20	chr1:78878600-78879200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr1:78878600-78880600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr1:78879000-78879600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr1:78879000-78879600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr1:78879200-78879400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr1:78879400-78880000	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr1:78879600-78879800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:78879600-78880000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr1:78879600-78880200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr1:78879600-78880600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:78879800-78884800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr1:78880000-78880600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr1:78880000-78881000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:78880400-78881000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr1:78880600-78880800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:78880600-78892000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr1:78881000-78884800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr1:78882400-78882600	Enhancers	NHDF-Ad	bronchial
38	chr1:78882600-78883800	Weak transcription	NHDF-Ad	bronchial
39	chr1:78883800-78884200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:78883800-78884800	Enhancers	NHDF-Ad	bronchial
41	chr1:78884200-78884400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:78884400-78884800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:78884600-78884800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:78884600-78884800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:78884600-78885400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:78884800-78885000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:78884800-78885000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr1:78884800-78885200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr1:78884800-78885200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:78884800-78885200	Flanking Active TSS	NHDF-Ad	bronchial

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